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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzenecarboximidamide, N-hydroxy-4-nitro-, (Z)-

ONC(=N)c1ccc(cc1)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzenecarboximidamide, N-hydroxy-4-nitro-, (Z)-
CAS Number: 1613-86-1
Product Number: AG001SBW(AGN-PC-0O4M12)
Synonyms:
MDL No:
Molecular Formula: C7H7N3O3
Molecular Weight: 181.1488

Identification/Properties

Properties
MP:
180℃
BP:
410.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
181.151g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
181.049g/mol
Monoisotopic Mass:
181.049g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
216
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Hydroxy-4-nitrobenzimidamide, a versatile compound widely employed in chemical synthesis, serves as a crucial building block in the creation of various organic compounds. Its unique structure, containing both a hydroxyl group and a nitro group on a benzimidazole ring, allows for a diverse range of reactions and functionalization strategies. In organic synthesis, N-Hydroxy-4-nitrobenzimidamide is frequently utilized as a key intermediate in the preparation of complex molecules, particularly in the development of pharmaceuticals, agrochemicals, and specialty chemicals. Through strategic manipulation of its chemical properties, researchers can access a plethora of derivatives with tailored characteristics and functionalities, making this compound an indispensable tool in modern synthetic chemistry.